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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 925449Generated: October 29, 2026

Furfural → HCID 89500527, compound

https://huagongshe.com/reaction/925449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFurfuralHCID 7362—
ReactantSodium AcetateHCID 517045—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 89500570HCID 89500570—
SolventMethanolHCID 887—
ProductHCID 89500527HCID 89500527—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of [5-(5-amino-2-fluoro-phenyl)-5-methyl-5,6-dihydro-2H-[1,4]oxazin-3-yl]-carbamic acid tert-butyl ester (77.5 mg, 0.240 mmol) and NaOAc (59.0 mg, 0.719 mmol) in MeOH (1 ml) was added 2-furaldehyde (0.020 ml, 23.0 mg, 0.240 mmol). The reaction mixture was degassed with Ar and stirred for 15 min at 100° C. in a microwave. After cooling to 0° C., NaBH4 (10.02 mg, 0.252 mmol) was added portionwise and stirring was continued at rt for 1 h. The reaction mixture was quenched with water and diluted with EtOAc. The phases were separated and the aq. layer was twice reextracted with EtOAc. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated. The resulting title compound was purified by FC (cyclohexane:EtOAc 100:0 to 80:20).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284284B2
Source datasetuspto-grants-2016_03
ORD IDord-83ef3cc1e16740d8ad3f34db97ab80c9
Source noteuspto-grants-2016_03